EXCLUSIVE: FDA lab uncovers excess DNA contamination in COVID-19 vaccines. Explosive revelations as a study conducted at FDA's own lab found residual DNA levels exceeded safety limits by 6 to 470 times. Experts say it's a 'smoking gun.' By Maryanne Demasi, PhD (01/02/25)
Quoted from the article:
An explosive new study conducted within the U.S. Food and Drug Administration’s (FDA) own laboratory has revealed excessively high levels of DNA contamination in Pfizer’s mRNA COVID-19 vaccine.
Tests conducted at the FDA’s White Oak Campus in Maryland found that residual DNA levels exceeded regulatory safety limits by 6 to 470 times.
The study was undertaken by student researchers under the supervision of FDA scientists. The vaccine vials were sourced from BEI Resources, a trusted supplier affiliated with the National Institute of Allergy and Infectious Diseases (NIAID), previously headed by Anthony Fauci.
The article then describes the methods, expert reaction, regulatory oversight under scrutiny, and implications for manufacturers and regulators.
Key Commentary:
→ Kevin McKernan — longtime genome researcher; former director of the Human Genome Project
“These findings are significant not just for what they reveal but for what they suggest has been concealed from public scrutiny. Why has the FDA kept these data under wraps?”
McKernan states that the study’s methods may have underestimated contamination levels. He also said:
“Chronic activation of the cGAS-STING pathway [a crucial component of the innate immune response] could paradoxically fuel cancer growth. Repeated exposure to foreign DNA through COVID-19 boosters may amplify this risk over time, creating conditions conducive to cancer development.”
“To assert that the DNA fragments are non-functional, they would need to transfect mammalian cells and perform sequencing, which wasn’t done here. Moreover, the methods used in this study don’t effectively capture the full length of DNA fragments. A more rigorous sequencing analysis could reveal SV40 fragments several thousand base pairs long, which would likely be functional.”
→ Nikolai Petrovsky — Professor of Immunology and director of Vaxine Pty Ltd.
“It clearly shows the FDA was aware of these data. Given that these studies were conducted in their own labs under the supervision of their own scientists, it would be hard to argue they were unaware.”
“The only practical solution is for regulators to require manufacturers to demonstrate that the plasmid DNA levels in the vaccines are safe. Otherwise, efforts to remove the residual DNA would result in an entirely new vaccine, requiring new trials and effectively restarting the process with an untested product.”
ED NOTE It's odd that the FDA allowed this study to be conducted. And by high school kids! We smell a lab rat.
